A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5877438



Internal ID9442662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:64331889..64344628hg38UCSC Ensembl
chr8:65244446..65257185hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3812740
hg1912740
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676031
Supporting Variants
SamplesNA18856
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5877438
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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